Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
  • C07C29/32—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring increasing the number of carbon atoms by reactions without formation of -OH groups
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
  • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
  • Y02P20/00—Technologies relating to chemical industry
  • Y02P20/50—Improvements relating to the production of bulk chemicals
  • Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts

Definitions

• the present invention relates to a process for the production of a product comprising ethanol by the liquid phase hydrocarbonylation of methanol.
• Ethanol is a valuable industrial product which is generally manufactured either by fermentation of natural products, e.g. molasses, or by hydration of ethylene in the presence of an acid catalyst such as phosphoric acid.
• the present invention provides a process for the production of a product comprising ethanol which process comprises reacting at elevated temperature and pressure and in the liquid phase methanol with hydrogen and carbon monoxide in the presence of an inert, particulate solid comprising a high surface area form of silica, alumina, silica/alumina or carbon, a methanol soluble homologation catalyst comprising either:
• Cobalt as the sole catalytic metal entity in the methanol soluble catalyst may be added as cobalt carbonyl.
• cobalt may be added in the form of bis(triphenylphosphine) iminium tetracarbonylcobaltate of formula [(C 6 H 5 ) 3 PNP(C 6 H 5 ) 3 ] + [Co(CO) 4 ],which is available commercially.
• the cobalt may also be added in a form capable of forming the carbonyl and/or a carbonyl/hydride complex under the prevailing reaction conditions.
• cobalt is preferably added in the ionic form, but the use of cobalt metal to react 'in situ' to form ionic cobalt which then further reacts to form the carbonyl and/or carbonyl/hydride complex is within the scope of the present invention.
• Typical sources of cobalt are, for example, compounds such as the carboxylate salt, e.g. the acetate,formate,propionate or the like, which under the reaction conditions form carbonyl or carbonyl/hydride complexes.
• the Group VIII metal may be added either as a metal complex in which the ligand is derived from cyclopentadiene or a substituted cyclopentadiene having the formula (I) or in a form capable of forming the complex under the prevailing reaction conditions.
• Suitable methods for preparing the metal complex are described in the aforesaid publication entitled 'Organometallic Compounds'.
• One such method is by the reaction, in tetrahydrofuran, of freshly prepared sodium, potassium or thallium is derived from cyclopentadiene or a substituted cyclopentadiene of formula: in which R is independently hydrogen, methyl or ethyl, or in a form capable of forming the complex under the prevailing reaction conditions, and a promoter comprising either an iodide or a bromide.
• ligand as used herein is defined in "Advanced Inorganic Chemistry” by F A Cotton and G Wilkinson, Wiley (US), 3rd edition 1972, which on page 139 defines a ligand as any atom, ion or molecule capable of functioning as the donor partner in one or more co-ordinate bonds.
• Methanol is a readily available industrial product. It is generally manufactured on an industrial scale from synthesis gas. Whilst it is preferred that the methanol be substantially pure the presence of small amounts of certain impurities can be tolerated. The methanol may however contain up to 50% by weight of water.
• synthesis gas Mixtures of the gases hydrogen and carbon monoxide are abundantly available in the form of synthesis gas.
• Methods for preparing synthesis gas are well known in the art and usually involve the partial oxidation of a carbonaceous substance, e.g. coal.
• synthesis gas may be prepared, for example, by thermal steam reforming of methane.
• the molar ratio of carbon monoxide to hydrogen may suitably be in the range 2:1 to 1:3, preferably 1:1 to 1:2.
• Methods for adjusting the molar ratio of carbon monoxide to hydrogen are well known to those versed in the art.
• substantially pure synthesis gas the presence of such impurities cyclopentadienide with an anhydrous Group VIII metal halide or other suitably soluble metal salt.
• the metal complex may be prepared 'in situ' under the prevailing reaction conditions by feeding a metal salt such as the halide with sodium, potassium or thallium cyclopentadienide.
• the iodide or bromide can be added either in ionic form or as molecular iodine (I 2 ) or bromine (Br 2 ) or as an alkyl or aryl iodide or bromide, preferably methyl iodide.
• the iodide or bromide may be added as metal iodide or metal bromide.
• the iodide or bromide may also be added in ionic form utilising cations which are inert with regard to the hydrocarbonylation reaction. Typical of the inert form is potassium iodide or bromide, sodium iodide or bromide and lithium iodide or bromide. Of the iodide or the bromide the iodide is preferred.
• the molar ratio of catalyst (i) or catalyst (ii) to the iodide or bromide may suitably be within the range from 1:5 to 10:1, preferably from 1:2 to 5:1.
• the inert particulate solid suitably has a surface area greater than 100, preferably greater than 200m2/g.
• Silica may be present in the form of powdered glass, silica gel or a diatomaceous earth of the type known as Fullers earth, e.g. kieselguhr. Carbon may be present, for example, in the form of graphite or charcoal.
• Alumina may be present either alone or combined with silica in the form of a zeolite having a silica to alumina molar ratio less than 12:1, such as a large pore size Y-type zeolite. Zeolites having a higher silica to alumina molar ratio, such as the ZSM-type zeolites, tend to dehydrate methanol and for this reason their use is not preferred.
• co-promoter is a compound having the general formula: wherein X is nitrogen, phosphorus, arsenic, antimony or bismuth and A, B and C are individually monovalent hydrocarbyl groups containing from 1 to 20 carbon atoms,which hydrocarbyl groups are free from aliphatic carbon - carbon unsaturation and are bound to the X atom by a carbon/X bond, or X is phosphorus, arsenic, antimony or bismuth and any two of A, B and C together form an organic divalent cyclic ring system bonded to the X atom, or X is nitrogen and all of A, B and C together form in organic trivalent cyclic ring system bonded to the X atom.
• Preferred compounds having the formula (II) are those in which X is nitrogen, phosphorus, arsenic, antimony or bismuth and A, B and C are independently monovalent hydrocarbyl groups.
• the hydrocarbyl groups may suitably be substituted or unsubstituted saturated aliphatic groups, saturated cycloaliphatic groups or aromatic groups, of which the unsubstituted groups are preferred.
• Examples of suitable compounds having the formula (II) are triphenylamine, triphenylphosphine, triphenylarsine, triphenylstibine, triphenylbismuth, triethylphosphine, tri-n-butylphosphine, tri-t-butylphosphine, tricyclohexylphosphine, tris (4-tolyl) phosphine, tris (3-chlorophenyl) phosphine, diphenylhexylphosphine, dibutyloctadecylphosphine, tribenzylphosphine, pyridine, diphenylamine and tri-n-butylarsine.
• Preferred compounds having the formula (II) are triphenylphosphine, triethylphosphine and tri-n-butylphosphine.
• the co-promoter may be a polydentate ligand wherein the donor atoms are either identical or combinations of dissimilar atoms of the elements nitrogen, phosphorus, arsenic, antimony or bismuth, with the proviso that no two of the atoms are directly bonded to each other.
• Suitable such polydentate ligands are described in the specification accompanying our copending published European application No: 79302053 (BP Case No: 4662).
• the polydentate ligand is a compound having the formula:- wherein X and Y are independently nitrogen, phosphorus, arsenic, antimony or bismuth, n is an integer, R 1 , R 2 , R 3 and R are independently hydrocarbyl groups containing from 1 to 20 carbon atoms as defined in the compound of formula (II) and R and R are either hydrogen atoms or hydrocarbyl groups containing from 1 to 20 carbon atoms as defined for the compound of formula (II).
• Illustrative of suitable compounds of formula (III) which may be used as component (iii) of the catalyst are (C 6 H 5 ) 2 P(CH 2 ) P(C 6 H 5 ) 2 ; (C 6 H 5 ) 2 P(CH 2 ) 4 P(C 6 H 5 ) 2 and (C 6 H 5 ) 2 )(CH 2 ) 6 P(C 6 H 5 ) 2 .
• the molar ratio of catalyst (i) or catalyst (ii) to the further promoter may suitably be in the range 1:1 to 1:10, preferably 1:1 to 1:3.
• hydrocarbyl has been used throughout the foregoing in its accepted meaning as representing a radical formed from a hydrocarbon by removal of a hydrogen atom.
• the elevated temperature may be in the range 150 to 250°C, preferably 180 to 230°C.
• the temperature may be in the range 145 to 210°C, preferably 170 to 195°C.
• the elevated pressure which may be used in the presence of catalyst (i) may be greater than 50 bars, preferably in the range 50 to 300 bars, and in the presence of catalyst (ii) the pressure may be in the range 1 to 300 bars, preferably 50 to 200 b d rs.
• the process may be carried out batchwise or continuously, continuous operation being preferred.
• a preferred method of operating the process continuously comprises continuously feeding synthesis gas and a liquid feed comprising methanol, catalyst(or compounds giving rise to the catalyst under the reaction conditions) and promoter or promoters to a reactor, suitably in tubular form, containing a bed of the inert, particulate solid maintained under conditions of elevated temperature and pressure and continuously removing from the reactor unreacted synthesis gas and a liquid product containing ethanol by products, unchanged methanol, catalyst and promoters.
• the unreacted synthesis gas may be separated and recycled to the reactor.
• the liquid product may be processed, suitably by distillation, to recover light ends including ethers, by-products, ethanol, unreacted methanol, catalyst and promoter(s).
• the methanol, catalyst and promoter(s) may be recycled to the reactor.
• the solid be employed in the form of a suspension or a bed it may suitably occupy up to 50% by volume of the reactor space.
• the residence time may suitably be up to 8 hours, but is preferably in the range of from 20 to 200 minutes. Short residence times are preferred because long residence times may lead to further reaction of acetaldehyde by aldol condensation-type reaction giving, for example, n-butyraldehyde.
• the residence time for batchwise operation is that time during which the reactor is at the specified reaction temperature. When the process is operated continuously the residence time is calculated as follows:-
• the methanol may contain up to 50% by weight of water.
• the molar ratio of methanol to synthesis gas fed in both continuous and batch operation may be in the range of from 10:1 to 1:20, preferably from 2:1 to 1:5.
• the molar ratio of catalyst (i) or catalyst (ii) to methanol may be in the range 1:10 to 1:1000, preferably from 1:4 to 1:800.
• the yield of realisable ethanol is defined as the yield of free ethanol plus the yield of ethanol realisable by the hydrolysis of ethanol-yielding esters (e.g. ethyl acetate).
• realisable methanol is defined as the free methanol plus the methanol realisable by the hydrolysis of methanol-yielding esters (e.g. methyl acetate).
• the yield of realisable acetic acid is meant the yield of free acetic acid plus the yield of acetic acid realisable by the hydrolysis of acetic acid-yielding esters (e.g. methyl acetate). In calculating the yield it is assumed that all the acetic acid is derived from methanol and synthesis gas.
• Catalyst A,particulate activated alumina A1 2 0 3 ; 2.25g
• the autoclave was pressured with a 1:1 mixture of carbon monoxide and hydrogen (to about 100 bars). The reactor temperature was rapidly raised to 205°C and the pressure adjusted.to 200 bars. After two hours the autoclave was cooled to room temperature and the reaction products analysed by gas- liquid chromotography (GLC). The reaction conditions and the yield of ethanol are shown in the following Table. GLC revealed that small amounts of dimethyl ether,acetaldehyde, n-butyraldehyde, carbon dioxide and methane were formed as by-products.
• Example 1 was repeated, except that particulate activated alumina (Al 2 O 3 ) was not added to the catalyst charge.
• Example 1 was repeated, but with the addition of.10 g of particulate activated charcoal to the catalyst charge in place of the activated alumina.
• Example 1 was repeated, but with the addition of 5 g of particulate kieselguhr to the catalyst charge in place of the activated alumina.
• Example 4 was repeated except that no particulate activated alumina was added to the catalyst charge.
• Catalyst C triphenylphosphine
• Example 5 was repeated except that no particulate activated alumina was added to the catalyst charge.
• Comparison Tests 1 to 3 are not examples in accordance with the present invention because they do not include an inert particulate solid and are included only for the purpose of comparison.

Landscapes

• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Applications Claiming Priority (2)

Publications (1)

Family

ID=10512162

Family Applications (1)

Country Status (4)

Cited By (1)

Families Citing this family (5)

Citations (1)

Family Cites Families (10)

• 1981
  • 1981-03-11 US US06/242,488 patent/US4357480A/en not_active Expired - Fee Related
  • 1981-03-11 EP EP81301023A patent/EP0036724A1/fr not_active Withdrawn
  • 1981-03-13 NZ NZ196496A patent/NZ196496A/xx unknown
  • 1981-03-18 JP JP3927581A patent/JPS56140938A/ja active Pending

Patent Citations (1)

Also Published As

Similar Documents

Legal Events